1.G.-Q. Chen, C. G. Daniliuc, G. Kehr, G. Erker*, “Making Use of the Functional Group Combination of a Phosphane/Borane Lewis Pair Connected by an Unsaturated Four-Carbon Bridge” Eur. J. Inorg. Chem. 2017, 4519-4524.
2.G.-Q. Chen, G. Kehr, C. G. Daniliuc, M. Bursch, S. Grimme, G. Erker*, “Intermolecular Redox-Neutral Amine C-H Functionalization Induced by the Strong Boron Lewis Acid B(C6F5)3 in the Frustrated Lewis Pair Regime" Chem. Eur. J. 2017, 23, 4723-4729.
3.G.-Q. Chen, G. Kehr, C. Mück-Lichtenfeld, C. G. Daniliuc, G. Erker*, “Phospha-Claisen type reactions at frustrated Lewis pair frameworks” J. Am. Chem. Soc. 2016, 138, 8554-8559.
4.G.-Q. Chen, G. Kehr, C. G. Daniliuc, C. Mück-Lichtenfeld, G. Erker*, “Formation of thermally robust frustrated Lewis pairs by electrocyclic ring closure reactions” Angew. Chem. Int. Ed. 2016, 55, 5526-5530.
5.G.-Q. Chen, G. Kehr, C. G. Daniliuc, G. Erker*, “Nitro-redox reactions at a frustrated borane/phosphane Lewis pair” Dalton. Trans. 2016, 45, 6820-6823.
6.G.-Q. Chen, F. Türkyilmaz, C. G. Daniliuc, C. Bannwarth, S. Grimme, G. Kehr, G. Erker*, “Enamine/butadienylborane cycloaddition in the frustrated Lewis pair regime” Org. Biomol. Chem. 2015, 13, 10477-10486.
7.G.-Q. Chen, G. Kehr, C. G. Daniliuc, B. Wibbeling, G. Erker*, “Bifunctional behavior of unsaturated intramolecular phosphane-borane frustrated Lewis pair derived from uncatalyzed 1,4-hydrophosphination of a dienylborane” Chem. Eur. J. 2015, 21, 12449-12455.
8.G.-Q. Chen, G. Kehr, C. G. Daniliuc, G. Erker*, “1,1-alkenylboration of diarylphosphino-enynes: convenient synthetic entry to vicinal P/B Lewis pairs at extended conjugated π-frameworks” Org. Biomol. Chem. 2015, 13, 764-769.
9.P. Moquist#, G.-Q. Chen#, C. Mück-Lichtenfeld, K. Bussmann, C. G. Daniliuc, G. Kehr, G. Erker*, “α-CH acidity of alkyl-B(C6F5)2 compounds – the role of stabilized borata-alkene formation in frustrated Lewis pair chemistry” Chem. Sci. 2015, 6, 816-825. (#contributed equally)
10.G.-Q. Chen, Z.-J. Xu, C.-Y. Zhou, C.-M. Che*, “Selective oxidation of terminal aryl and aliphatic alkenes to aldehydes catalyzed by iron(III) porphyrins with triflate as a counter anion” Chem. Commun. 2011, 47, 10963-10965.
11.G.-Q. Chen, Z.-J. Xu, Y. Liu, C.-Y. Zhou, C.-M. Che*, “Iron-catalyzed nitrene insertion reaction for facile construction of amide compounds” Synlett 2011, 1174-1178.
12.G.-Q. Chen, Z.-J. Xu, S. L.-F. Chan, C.-Y. Zhou, C.-M. Che*, “Homogeneous silver(I) salts and heterogeneous Ag3PW12O40-catalyzed intermolecular allylation of arenes with allylic alcohols” Synlett 2011, 2713-2718.
13.T. Özgün, G.-Q. Chen, C. G. Daniliuc, A. C. McQuilken, T. H. Warren, R. Knitsch, H. Eckert, G. Kehr, G. Erker*, “Unsaturated vicinal frustrated Lewis pair formation by electrocyclic ring closure and their reaction with nitric oxide” Organometallics 2016, 35, 3667-3680.
14.Y. Liu, G.-Q. Chen, C.-W. Tse, X. Guan, Z.-J. Xu, J-S. Huang, C.-M. Che*, “[Fe(F20TPP)Cl]-catalyzed amination with arylamines and {[Fe(F20TPP)(NAr)](PhI=NAr)}+. intermediate assessed by high-resolution ESI-MS and DFT calculations” Chem. Asian. J. 2015, 10, 100-105.
15.T. W.-S. Chow, G.-Q. Chen, Y. Liu, C.-Y. Zhou, C.-M. Che*, “Practical iron-catalyzed atom/group transfer and insertion reactions” Pure Appl. Chem. 2012, 84, 1685-1704.
